Author

Mohammed Alkhanafsa

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Open access 2026

Isolated Severe Prolongation of Prothrombin Time Revealing Congenital Factor VII Deficiency With Mild Bleeding Phenotype: A Case Report

Congenital Factor VII (FVII) deficiency is a rare inherited bleeding disorder characterized by marked variability in bleeding severity and poor correlation between factor activity levels and clinical phenotype. We report a 21-year-old woman who presented with recurrent spontaneous ecchymoses without mucosal bleeding, m...

Mohammed Alkhanafsa, O. Mosleh, Jamil Wafi et al. · Yemen Journal of Medicine · 0 citations

Open access Sep 2026

Clinical Deterioration Among Emergency Department Boarders: From Hallway Monitoring to a Structured Rescue System

Background: Emergency department (ED) boarding places admitted patients in an environment designed for rapid episodic assessment rather than longitudinal inpatient surveillance. The resulting mismatch in ownership, monitoring, medication delivery, fundamental nursing care, and rescue capability creates a clinically imp...

Mohammed Alkhanafsa, Jamil Wafi, Soud M. S. Deek · Panorama of Emergency Medici... · 0 citations

Review Open access 2026

A Rare Case of Adult-Onset Acute Disseminated Encephalomyelitis Presenting with Seizure and Acute Confusion: A Case Report and Literature Review

Acute disseminated encephalomyelitis (ADEM) is an immune-mediated inflammatory demyelinating disorder of the central nervous system, typically encountered in the pediatric population. Adult-onset ADEM is uncommon and poses a diagnostic challenge, particularly when presenting with seizure as a cardinal feature and when...

Mohammed Alkhanafsa, Jamil Wafi, O. Mosleh et al. · Yemen Journal of Medicine · 0 citations